Cooperation of hTERT, SV40 T antigen and oncogenic Ras in tumorigenesis: A cell transplantation model using bovine adrenocortical cells

Michael Thomas, Tetsuya Suwa, Lianqing Yang, Lifang Zhao, Christina L. Hawks, Peter J. Hornsby

Research output: Contribution to journalArticle

25 Scopus citations


Expression of TERT, the reverse transcriptase component of telomerase, is necessary to convert normal human cells to cancer cells. Despite this, "telomerization" by hTERT does not appear to alter the normal properties of cells. In a cell transplantation model in which bovine adrenocortical cells form vascularized tissue structures beneath the kidney capsule in scid mice, telomerization does not perturb the functional tissue-forming capacity of the cells. This cell transplantation model was used to study the cooperation of hTERT with SV40 T antigen (SV40 TAg) and oncogenic Ras in tumorigenesis. Only cells expressing all three genes were tumorigenic; this required large T, but not small t, antigen. These cells produced a continuously expanding tissue mass; they were invasive with respect to adjacent organs and eventually destroyed the kidney. Cells expressing only hTERT or only Ras produced minimally altered tissues. In contrast, SV40 TAg alone produced noninvasive nodules beneath the kidney capsule that had high proliferation rates balanced by high rates of apoptosis. The use of cell transplantation techniques in a cell type that is able to form tissue structures with or without full neoplastic conversion allows the phenotypes produced by individual cooperating oncogenes to be observed.

Original languageEnglish (US)
Pages (from-to)493-500
Number of pages8
Issue number6
StatePublished - Jan 1 2002



  • Adrenal cortex
  • Cell transplantation
  • Oncogenic Ras
  • SV40 T antigen
  • Telomerase

ASJC Scopus subject areas

  • Cancer Research

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